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  4. Engineering of a high lipid producing Yarrowia lipolytica strain

Engineering of a high lipid producing Yarrowia lipolytica strain

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sword-2019-09-12T12:28:25.original.xml (130 B)
Original SWORD entry document
Author(s)
Friedlander, Jonathan
•
Tsakraklides, Vasiliki
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Kamineni, Annapurna
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Greenhagen, Emily H.
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Consiglio, Andrew L.
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MacEwen, Kyle
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Crabtree, Donald V.
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Afshar, Jonathan
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Nugent, Rebecca L.
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Hamilton, Maureen A.
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Date Issued
March 2016
Journal
Biotechnology for Biofuels
Publisher
Springer Nature
Citation
Friedlander, Jonathan, Vasiliki Tsakraklides, Annapurna Kamineni et al. "Engineering of a high lipid producing Yarrowia lipolytica strain" Biotechnology for Biofuels, 9,77 (March 2016): p. 1-12. © 2016 Friedlander et al.
Version
Final published version
Abstract
Background: Microbial lipids are produced by many oleaginous organisms including the well-characterized yeast Yarrowia lipolytica, which can be engineered for increased lipid yield by up-regulation of the lipid biosynthetic pathway and down-regulation or deletion of competing pathways. Results: We describe a strain engineering strategy centered on diacylglycerol acyltransferase (DGA) gene overexpression that applied combinatorial screening of overexpression and deletion genetic targets to construct a high lipid producing yeast biocatalyst. The resulting strain, NS432, combines overexpression of a heterologous DGA1 enzyme from Rhodosporidium toruloides, a heterlogous DGA2 enzyme from Claviceps purpurea, and deletion of the native TGL3 lipase regulator. These three genetic modifications, selected for their effect on lipid production, enabled a 77 % lipid content and 0.21 g lipid per g glucose yield in batch fermentation. In fed-batch glucose fermentation NS432 produced 85 g/L lipid at a productivity of 0.73 g/L/h. Conclusions: The yields, productivities, and titers reported in this study may further support the applied goal of cost effective, large -scale microbial lipid production for use as biofuels and biochemicals. Keywords: Yarrowia lipolytica, Lipid accumulation, Oleaginous yeast, Metabolic engineering
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
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Creative Commons Attribution 4.0 International license
https://creativecommons.org/licenses/by/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/125833
DOI of Published Version
https://doi.org/10.1186/S13068-016-0492-3
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